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Concentration gradient
region along which concentration changes and can be across a membrane (abrupt)
Electrochemical gradient
separation of ions across a membrane (usually 1+ ion)
-Difference in charge + chemicals
membrane potential
electrical charge difference across a membrane
-can be measured in millivolls (mV)
What is the membrane potential of a resting cell?
-70 to -90mV
Diffusion
Because of motion, molecules spread out to fill space (High to low conentration)
Osmosis
move from:
-High [water] to low [water]
-Low [solute] to high [solute]
Reverse osmosis
way to purify water
Tonicity
hypertonic, hypotonic, isotonic
Isotonic
same

Hypertonic
Crenate = shrink

Hypotonic
Lyse = swell

Two types of Passive transport? (require no energy)
1. Simple Diffusion
2. Facilitated Diffusion
Simple Diffusion
substances passes directly through lipid bilayer (High to low)
-osmosis
Facilitated Diffusion
Substance needs help to pass through membrane by channel or carrier proteins (High to low)
Active Transport
needs energy (ATP) and protein pumps (Low to high) against gradient
-Na+/K+ pump
Na+/K+ pump
pumps 3Na+ out and 2K+ in
-separation of ions
-separation of charge= 1+ out in extracellular fluid

Does Active transport have potential energy?
Yes. Active transport goes uphill and [] gradient contains potential energy
-energy can be stored in a gradient
-chemical energy (ATP) to gradient
Co-transport
transport of 2+ more solutes at same time
-usually couples "down gradient" transport to "against gradient"
-requires cotransporter protein
-can be symporter or antiporter
Secondary Active Transport
Energy stored in Na+ gradient from ATP and used to transport solute against gradient (ex. glucose)
Bulk Transport (vesicles)
little membrane bubbles inside cell (phospholipids) to transport stuff
-microtubules are train tracks for intracellular vesicle transport
-kinesin (motor molecules) pulling a vesicle
Exocytosis
releasing stuff to outside
-secretion (insulin)
-vesicle fuse w/ membrane
Endocytosis
Bring stuff into cell
-large molecules and particles
3 types of endocytosis
1. Pinocytosis = cell drinking (contents of vesicle are random)
2. Phagocytosis = cell eating food vacuole (pseudopodia extend around food)
3. Receptor-mediated = receptors on cell surface grab target molecules (receptors collected in vesicle and collect specific molecules)
DNA
-monomer= nucleotide
-Nitrogeneous bases= Deoxyribose
-sugar: A,T,C,G
-double stranded
-Directionality in nucleic acids= phosphate end is 5' and Free OH- end is 3'
(synthesis 5'to3' new nucleotides added to 3')
RNA
-monomer= nucelotides
-N bases= ribose
-Sugar= A,U,C,G
- 1 strand and sometimes wrap around
DNA strands are parallel or antiparallel?
Antiparallel because strands run in opposite directions and form a double helix
Chromatin
chromatin fibers (DNA + proteins)
-placed into a chromosome during cell division
chromosome
1 DNA molecule + proteins
Centromere
narrow part of chromosome near middle

Describe human chromosomes
46 per cell= 2 sets of 23
-44 autosomes = 2 sex chromsomes
-XX = female
-XY= male
Genome
all the genetic information in a cell or in an organism
genomics
study of genome (human genome project= 13 years)
Ribosome
made of proteins and RNA
-site of protein synthesis
-free in cytoplasm or bound to nuclear envelope or RER
How is polypeptide made?
DNA to RNA to protein
-Info in DNA (a gene) transferred to messenger RNA
-mRNA moves out of nucleus
-Ribosome moves along mRNA translating genetic info to amino acid sequence
-Polypeptide is threaded into ER from ribosome
Gene
unit of hereditary
-segments of DNA (genetic info + codes for an RNA product)
-mRNA, tRNA, rRNA
-1 mRNA makes 1 polypeptide
-1 gene makes 1 kind of polypeptides
Hemoglobin is made of 4 polypeptides: 2 identical alpha chains and 2 identical beta chains. How many genes are required to make hemoglobin?
3
Gene expression
Turning info into DNA into working protein
-a gene doesn't directly make a polypeptide
-is made in cytoplasm
-RNA intermediate carries info (mRNA)
Explain process of transcription
synthesis of RNA from info in DNA
-DNA strand= template strand
RNA polymerase = enzyme that reads template strand
-Pre-mRNA converted to final functional form (cap and tail splicing)
-nuclear pore allows mRNA to make polypeptide
-ribosome uses info in mRNA to make polypeptide (reads mRNA and adds appropriate AA one at a time)
genetic code
sequence of 3 bases designate AAs
Codon
triplet code
-codons read by the ribosome 5' to 3' on mRNA
-each codon specifies next AA
-redundancy
-not ambiguous: no codon codes for 2 AAs
-special codons
-stop codons
RNA processing
pre-mRNA to mRNA
-5' cap added to 5' end (modified guanine nucleotide)
-poly-A tail= an enzyme adds 50-250 A's to 3' end
Explain exons and introns
-exons = segments that code for AA
-introns = intervening sequences that do not code
-introns cut out and exons connected together
-alternatice splicing = sometimes not all exons used and cell can put different exons together in different ways
tRNA
transfer RNA (AAs to ribosome)
describe translation process
-AAs covalently link to appropriate tRNA
-tRNA match with mRNA codons on the ribosome and add AA to growing chain
-Ribosome moves alon mRNA codon by codon
Ribosome
-large and small subunit only together when bond to mRNA
-3 binding sites: A-site= entry point for tRNA bringing next AA P-site= holds tRNA connected to polypeptide E-site= exit
What are the stages of translation? (photo in notebook)
1. Initiation
2. Elongation
3. Termination
Describe the Initiation stage of translation
-Ribosomes and 1st tRNA bind to mRNA at start codon
Describe the elongation stage of translation
tRNA enters A-site and binds to codon
-growing chain transferred to A site
-New peptide bond formed
-ribosome shifts to next codon and tRNA shift position (old tRNA leaves)
Describe the termination stage of translation
Release factor = protein that binds to stop codon
Overall summary of gene expression
Inside nucleus:
Transcription
-RNA polymerase turnes DNA to mRNA
-Splicing happens (introns out just exons)
-Tail---mRNA---Cap
Outside nucleus:
Translation
-AA attachment
-Initiation, Elongation, Termination
-polypeptide
Housekeeping genes
always expressed (Constant levels) basic metabolic function, structure, etc.
-ex: cytoskeleton proteins (actin and tubulin)
Inducible genes
can be turned on and off and expression levels can be varied as needed
-Ex: iNOs (inducible nitric oxide synthase during inflammation)
Tissue specific expression
liver specific genes only turned on in lover but all genes present
-Ex: hemoglobin (only RBA) Pepsin (only chief cells in stomach)
Example of inducible gene
-hormone= prolactine
-target= mammary gland cells
-prolactine to casein gene expression (milk protein)
1. prolactine binds to receptor
2. signal is carried by signaling cascade (regulatory protein phosphorylated)
3. regulatory protein enters nucleus (binds to DNA near casein gene and turns it on)
4. transcription
5. mRNA leaves nucleus (Bound ribosome threads polypeptide into RER and is processed, collected in vesicles, sent to golgi)
6. Golgi finishing touches (secretory vesicles)
7. Exocytosis into mammary gland duct
Why do cells divide?
Growth, replacement, healing
Explain why DNA must duplicate before division
Starts with 1 set of DNA, 2 copies of DNA, 2 daughter cells with 1 copy each
DNA copying
replication
Explain process of duplicating DNA
1. Double helix unzips into template for new strands
2. nucleotides added 1 by 1 (base pairing with template and DNA polymerase)
3. Begins at origin of replication (multiple origins per chromosome in humans)
4. Replication bubble forms as DNA unzips (spread out until merge)
Cell cycle
-Sequence of events from formation of cell to its own division
-Has varying lengths (1 day, less, some not at all)
What are the three stages of cell cycle
1. Interphase
2. Mitotic phase
3. Cytokinesis
Describe interphase
-Takes up most of cell cycle
-Metabolism and growth
-3 phases:
1. G1 phase = normal cell functions
2. S phase = DNA synthesis
3. G2 phase = prep to divide
Describe mitotic division
-Division of the nucleus to equal distribution of chromosomes
-Has 4 phases:
1. Prophase
2. Metaphase
3. Anaphase
4. Telophase
Describe cytokinesis
-Division of cytoplasm
-Usually starts with anaphase/ telophase
-Cleavage furrow forms
-Contractile ring pinches cell in 2 (proteins)
-Results in 2 identical cells with some number of chromosomes
What is the G0 phase?
-The exit cell cycle at G1 some cells can re-enter
-Normal cell functions and no division
Spindle apparatus
made of microtubules and centrosomes + guides and separates chromosomes

Describe prophase
-Chromatin condense to chromosomes
-Mitotic spindle forms
-nuclear envelope disintegrates

Describe metaphase
-Chromosomes line up on plane in center of cell

Describe anaphase
-Duplicate chromosomes pulled apart by mitotic spindle towards opposite sides

Describe telophase
- Chromosomes uncoil and become chromatin
- Nuclear envelope forms
- Mitotic spindle disappears

Cell checkpoints
-wait until good to go
-Check to see if nutrients good, cell size, DNA ok?
-Growth factors for G1: signaling proteins to go
Cancer
disease of cell cycle control, uncontrolled cell division, and never cease division
-single cells get mutated
HeLa cells
Taken from Henrietta locks in 1951
-cervical cancer
-still alive today
-have been used in 1000s of experiments
What does the immune system do for cancer cells?
-Immune system often kills abnormal cells
-If cells evade the immune system then it creates a tumor
Benign tumor
Abnormal cell remain at original site and rarely deadly but can disrupt organs
Malignant tumor
Can spread through blood or lymph (metastasis) and tumors can disrupt organ function
Chemotherapy
use of cells to kill cancer cells
-many disrupt mitosis
-taxol freezes mitotic spindle
-vinblastine prevents spindle from forming
-estoposide blocks DNA replication
Histology in med takes place where
pathology lab
What are the three ways for histology in med
-Study of tissues
1. Biopsy
2. Histologist (prepare slides)
3. Pathologist (diagnose)
Microtome
super thin slides and have many different stains
Tissue
group of cells that function together to carry out specialized activities
-usually have a common origin in an embryo
Extracellular matrix (ECM)
made of proteins and polysaccharides
-is flexible, cushions, protects, resists forces, and connects cells
Collagen
most abundant protein in mammals and major component of ECM
-Strong fibers and made of 3 polypeptides (coiled coil)
what are the four types of tissues
1. Epithelial (sheet of cells)
2. Connective (few cells + lots of ECM)
3. Muscle (contractile)
4. Nervous (excitable to signals)
Epithelial tissues
Sheets of cells directly compacted and simple that have linings, coverings, protection, secretion, absorption, and filtration
Connective Tissue
Cells that have relatively few space
-Have a matrix (1 protein and ground substance)
protein fibers
collagen and elastic fibers
ground substance
stuff in between cells + fibers, often water + polysaccharides, hydroxyapatite, depends on tissue
What are three unexpected connective tissue?
Blood, bone, fat
excitability
membranes carry waves of electrical signals (membrane potential)
Neurons (nerve cells)
Receive + send electrical signals and integrrate information
Describe the structure of a neuron
- Has a cell body = soma = neurosoma (nucleus + organelles)
-several dendrites that receive signals
-axons that send signals

Neuroglia
Supporting cells that protect and nurture neurons (glia + glial cells)
What are the three types of muscle tissue
(contractile) skeletal, cardiac, smooth
Describe skeletal muscle
Muscle fibers (muscle cells/ myocytes) multinucleate, striations, voluntary
-Biceps brachii, rectus femoris, external anal sphincter
Describe smooth muscle
Involuntary, small cells, fusiform, often sheets of muscle in organ walls
-Arrector pili, walls of arteries, internal anal sphincter
Describe cardiac muscle
Cardiomyocytes, involuntary, branches, connected by intercalated discs
Cell junctions
cells connecting to other cells and ECM
Tight junctions
seals between cells and can be selectively permeable or not permeable
Adherens junctions
Holds cells together, cadherins, connect to microfilaments (adhesion belt)
Desmosomes junctions
Hold cells together, cadherins, connect to intermediate filaments